Decode the Genome
Advanced genomic intelligence platform. Enter a gene symbol, condition, or SNP ID (rs...) to explore the blueprint of life.
ゲノムインテリジェンスプラットフォーム
GenoMirai REST API
Integrate genomic intelligence directly into your applications. Query our curated variant database and SNPedia in real-time with a simple, predictable JSON API.
Search the local variant database by gene symbol, condition name, or clinical significance keyword. Supports pagination.
Proxy SNPedia data for a given rs identifier. Returns raw wiki content that can be parsed client-side for full variant annotations.
Returns live database statistics: total variant count, top genes by frequency, significance breakdown, and API health status.
Self-documenting endpoint. Returns a machine-readable JSON schema describing all available endpoints, parameters, and rate-limit information.
| Plan | Requests / min | Max results | SNPedia proxy | |
|---|---|---|---|---|
| Free | 60 | 50 per page | ✓ | Active |
| Pro | 600 | 100 per page | ✓ | Coming soon |
| Enterprise | Unlimited | Unlimited | ✓ + priority cache | Contact us |
Questions? Contact us at api@genomirai.jp
About GenoMirai
We believe that genomic data should be accessible, interpretable, and actionable — for researchers, clinicians, and curious minds alike.
GenoMirai (ゲノム未来 — "Genome Future") was founded in Tokyo, Japan in 2025 by Jorge Remón García and the team behind Dicra.io. The platform was born from a simple frustration: genomic data existed in abundance, but the tools to explore it remained fragmented, inaccessible, and designed only for specialists.
We built GenoMirai to bridge that gap — combining curated clinical variant databases with real-time SNPedia integration, wrapped in an interface that doesn't require a bioinformatics PhD to use.
Our multidisciplinary team brings together expertise in artificial intelligence, bioinformatics, full-stack engineering, and precision medicine. We're headquartered in Tokyo with contributors across Madrid and Barcelona.
GenoMirai is part of the Dicra ecosystem of technology products designed to democratize access to complex, high-value information — from genomics to language learning to blockchain infrastructure.
Every variant in our database traces back to peer-reviewed sources. We display clinical significance categories exactly as curated by ClinVar and SNPedia.
The core GenoMirai platform and API are free. Genomic knowledge should not be locked behind paywalls — it belongs to humanity.
From search performance to UI clarity, every decision is guided by one principle: help users reach accurate genomic insights as quickly as possible.